Package 83324-092-24
Brand: cold and flu severe day and night
Generic: acetaminophen, chlorpheniramine maleate, dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloridePackage Facts
Identity
Package NDC
83324-092-24
Digits Only
8332409224
Product NDC
83324-092
Description
1 KIT in 1 CARTON (83324-092-24) * 8 TABLET, COATED in 1 BLISTER PACK * 8 TABLET, COATED in 1 BLISTER PACK
Marketing
Marketing Status
Brand
cold and flu severe day and night
Generic
acetaminophen, chlorpheniramine maleate, dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"spl_id": "1d8bb148-461a-3efa-e063-6394a90ad4fc", "openfda": {"rxcui": ["1086991", "1110988", "2634819"], "spl_set_id": ["9b74dd00-8f84-4fce-b5ea-df886b595326"], "manufacturer_name": ["CHAIN DRUG MARKETING ASSOCIATION, INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (83324-092-24) * 8 TABLET, COATED in 1 BLISTER PACK * 8 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "83324-092-24", "marketing_start_date": "20240718"}], "brand_name": "Cold and Flu Severe Day and Night", "product_id": "83324-092_1d8bb148-461a-3efa-e063-6394a90ad4fc", "dosage_form": "KIT", "product_ndc": "83324-092", "generic_name": "Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride", "labeler_name": "CHAIN DRUG MARKETING ASSOCIATION, INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cold and Flu Severe Day and Night", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240718", "listing_expiration_date": "20261231"}